Date of Award
Fall 2009
Document Type
Thesis
Degree Name
Master of Science (MS)
Department
Chemistry & Biochemistry
Program/Concentration
Chemistry
Committee Director
Balasubramanian Ramjee
Committee Member
Patrick hatcher
Committee Member
Paula Mazzer
Committee Member
Jennifer Poutsma
Call Number for Print
Special Collections LD4331.C45 K35 2009
Abstract
Synthesis of morphologically distinct polymeric nanostructures is vital for their wide ranging applications from nanomedicine to material science. Among various polymeric nanostructures, nanocapsules in particular have attracted a lot of attention as nanoreactors and drug delivery vehicles in nanomedicine. Often, synthesis of nanocapsules is achieved by template-based approaches. A direct, template-free method for the fabrication of nanocapsules and a variety of other morphologically distinct polymeric architectures was developed. The photopolymerization of a resorcinarene thiol-ene surfactant in various solvents lead to the formation of nanocapsules, nanoparticles, fibers, distorted honeycomb-like lattices, and sheets. The progress of the polymerization reaction and the morphology of the resulting photopolymers were characterized by a battery of analytical techniques, including IR, NMR, TEM, SEM, EDS and DLS. Further, the influence of polymerization duration, monomer concentration, and oxygen in the formation of nanocapsules was evaluated. A photopolymerization-based one-pot synthesis and surface-functionalization method was developed by exploiting the residual thiol and ene functional groups present in the nanocapsules. To understand the importance of structural elements in the resorcinarene thiol-ene surfactant, a number of photopolymerization reactions involving various resorcinarene-ene surfactant and multithiols were also carried out.
Rights
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DOI
10.25777/a5aq-kh51
Recommended Citation
Kalaitzis, Zaharoula M..
"Solvent Dependent Morphologies in Thiol-ene Photopolymerization: A Facile Route to Synthesis of Resorcinarene Nanocapsules"
(2009). Master of Science (MS), Thesis, Chemistry & Biochemistry, Old Dominion University, DOI: 10.25777/a5aq-kh51
https://digitalcommons.odu.edu/chemistry_etds/124